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Familial hemiplegic migraine.
Villar-Martinez MD, Moreno-Ajona D, Goadsby PJ. Villar-Martinez MD, et al. Handb Clin Neurol. 2024;203:135-144. doi: 10.1016/B978-0-323-90820-7.00007-0. Handb Clin Neurol. 2024. PMID: 39174245 Review.
Hemiplegic migraine consists of attacks of migraine with aura that includes reversible motor weakness. ...The most described subtypes of familial hemiplegic migraine include FHM1, FHM2, and FHM3. These have been demonstrated …
Hemiplegic migraine consists of attacks of migraine with aura that includes reversible motor weakness. .. …
Familial Hemiplegic Migraine.
Jen JC. Jen JC. 2001 Jul 17 [updated 2024 Jul 4]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. 2001 Jul 17 [updated 2024 Jul 4]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. PMID: 20301562 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Familial hemiplegic migraine (FHM) falls within the category of migraine with aura. In migraine with aura (including FHM) the neurologic symptoms of aura are unequivocally localizable …
CLINICAL CHARACTERISTICS: Familial hemiplegic migraine (FHM) falls within the category of migraine with …
Hemiplegic migraine.
de Boer I, Hansen JM, Terwindt GM. de Boer I, et al. Handb Clin Neurol. 2024;199:353-365. doi: 10.1016/B978-0-12-823357-3.00015-X. Handb Clin Neurol. 2024. PMID: 38307656 Review.
Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which the aura phase includes transient motor weakness. ...The most important diagnostic tools remain a patient interview, neurological examination during attacks, and ex …
Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which the aura phase includes …
Diagnostic and therapeutic aspects of hemiplegic migraine.
Di Stefano V, Rispoli MG, Pellegrino N, Graziosi A, Rotondo E, Napoli C, Pietrobon D, Brighina F, Parisi P. Di Stefano V, et al. J Neurol Neurosurg Psychiatry. 2020 Jul;91(7):764-771. doi: 10.1136/jnnp-2020-322850. Epub 2020 May 19. J Neurol Neurosurg Psychiatry. 2020. PMID: 32430436 Free PMC article. Review.
Hemiplegic migraine (HM) is a clinically and genetically heterogeneous condition with attacks of headache and motor weakness which may be associated with impaired consciousness, cerebellar ataxia and intellectual disability. ...Mutations in CACNA1A, ATP1A2 …
Hemiplegic migraine (HM) is a clinically and genetically heterogeneous condition with attacks of headache and motor weakness w …
Exploring the association between familial hemiplegic migraine genes (CACNA1A, ATP1A2 and SCN1A) with migraine and epilepsy: A UK Biobank exome-wide association study.
Staehr C, Nyegaard M, Bach FW, Rohde PD, Matchkov VV. Staehr C, et al. Cephalalgia. 2025 Jan;45(1):3331024241306103. doi: 10.1177/03331024241306103. Cephalalgia. 2025. PMID: 39781574 Free article.
BACKGROUND: Familial hemiplegic migraine (FHM) types 1-3 are associated with protein-altering genetic variants in CACNA1A, ATP1A2 and SCN1A, respectively. ...A machine learning-based approach was employed to predict whether variants resul …
BACKGROUND: Familial hemiplegic migraine (FHM) types 1-3 are associated with protein-altering genetic variants in CA …
Hemiplegic Migraine.
Kumar A, Samanta D, Emmady PD, Arora R. Kumar A, et al. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 30020674 Free Books & Documents.
Hemiplegic migraine is a rare subtype of migraine with aura, characterized by the presence of motor weakness as an aura manifestation at the time of migraine attack. ...Familial Hemiplegic Migraine (FHM) FHM is …
Hemiplegic migraine is a rare subtype of migraine with aura, characterized by the presence of motor weakn …
Epilepsy in patients with familial hemiplegic migraine.
Hasırcı Bayır BR, Tutkavul K, Eser M, Baykan B. Hasırcı Bayır BR, et al. Seizure. 2021 May;88:87-94. doi: 10.1016/j.seizure.2021.03.028. Epub 2021 Mar 31. Seizure. 2021. PMID: 33839563 Free article. Review.
OBJECTIVE: The coexistence of epilepsy in familial hemiplegic migraine (FHM) has not been reviewed systematically. We investigated the associations of epilepsy in patients with FHM with CACNA1A, ATP1A2, SCN1A or PRRT2 mutations along with …
OBJECTIVE: The coexistence of epilepsy in familial hemiplegic migraine (FHM) has not been reviewed systematically. We i …
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
Romozzi M, Primiano G, Rollo E, Travaglini L, Calabresi P, Servidei S, Vollono C. Romozzi M, et al. J Headache Pain. 2021 Jul 28;22(1):85. doi: 10.1186/s10194-021-01297-5. J Headache Pain. 2021. PMID: 34320921 Free PMC article.
BACKGROUND AND AIMS: Hemiplegic migraine (HM) is a rare form of migraine characterized by the presence of a motor and other types of aura. HM can be sporadic or familial. Familial hemiplegic migraine (FHM) is an autosomal do …
BACKGROUND AND AIMS: Hemiplegic migraine (HM) is a rare form of migraine characterized by the presence of a motor and o …
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Hiekkala ME, Vuola P, Artto V, Häppölä P, Häppölä E, Vepsäläinen S, Cuenca-León E, Lal D, Gormley P, Hämäläinen E, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Harno H, Havanka H, Keski-Säntti P, Färkkilä M, Palotie A, Wessman M, Kaunisto MA, Kallela M. Hiekkala ME, et al. Cephalalgia. 2018 Oct;38(12):1849-1863. doi: 10.1177/0333102418761041. Epub 2018 Feb 27. Cephalalgia. 2018. PMID: 29486580
Objective To study the position of hemiplegic migraine in the clinical spectrum of migraine with aura and to reveal the importance of CACNA1A, ATP1A2 and SCN1A in the development of hemiplegic migraine in Finni …
Objective To study the position of hemiplegic migraine in the clinical spectrum of migraine with aura and …
Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation.
Martínez E, Moreno R, López-Mesonero L, Vidriales I, Ruiz M, Guerrero AL, Tellería JJ. Martínez E, et al. Case Rep Neurol Med. 2016;2016:3464285. doi: 10.1155/2016/3464285. Epub 2016 Oct 13. Case Rep Neurol Med. 2016. PMID: 27818813 Free PMC article.
Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor weakness during the aura phase. Mutations in CACNA1A, ATP1A2, SCN1A, and PRRT2 genes have been described. Metho …
Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attacks with motor …
84 results